Alcohols and polyols
- (1)
- (55)
- (347)
- (41)
- (4)
- (8)
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- (55)
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- (18)
- (1)
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- (156)
- (1)
- (64)
- (28)
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- (1)
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- (10)
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- (30)
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- (399)
- (6)
- (102)
- (22)
- (50)
- (31)
- (63)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
- (6)
- (13)
- (148)
- (116)
- (8)
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- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
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- (21)
- (5)
- (2)
- (2)
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- (16)
- (2)
- (30)
- (1)
- (4)
- (1)
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- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (15)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (5)
- (4)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (6)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
- (4)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (1)
- (4)
- (2)
- (3)
- (2)
- (4)
- (3)
- (1)
- (4)
- (5)
- (1)
- (4)
- (5)
- (9)
- (1)
- (5)
- (5)
- (2)
- (1)
- (1)
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- (5)
- (3)
- (5)
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- (11)
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- (10)
- (1)
- (1)
- (1)
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- (4)
- (11)
- (1)
- (2)
- (4)
- (20)
- (21)
- (2)
- (8)
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- (3)
- (3)
- (1)
- (8)
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- (1)
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- (1)
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- (1)
- (1)
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- (12)
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- (1)
- (1)
- (1)
- (7)
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- (1)
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- (1)
- (1)
- (5)
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- (3)
- (1)
- (1)
- (4)
- (6)
- (1)
- (1)
- (1)
- (5)
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- (1)
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- (1)
- (1)
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- (1)
- (1)
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- (5)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (14)
- (1)
- (1)
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- (1)
- (1)
- (4)
- (5)
- (2)
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- (1)
- (10)
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- (5)
- (1)
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- (5)
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- (1)
- (1)
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- (7)
- (1)
- (18)
- (16)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (82)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
- (19)
- (1)
- (22)
- (16)
- (1)
- (2)
- (21)
- (2)
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- (1)
- (67)
- (1)
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- (7)
- (4)
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- (1)
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- (72)
- (3)
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- (237)
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- (2)
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- (21)
- (279)
- (17)
- (1)
- (6)
- (280)
- (28)
- (2)
- (25)
- (2)
- (3)
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- (2)
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- (48)
- (3)
- (418)
- (6)
- (3)
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- (47)
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- (3)
- (1)
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- (21)
- (16)
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- (11)
- (1)
- (8)
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- (733)
- (11)
- (3)
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- (66)
- (2)
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- (33)
- (2)
- (31)
- (39)
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Filtered Search Results
Medchemexpress LLC Midodrine (hydrochloride) | 43218-56-0 | 99.9% | 25 MG
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Midodrine hydrochloride is a selective and orally active adrenergic α1-receptor agonist. It strengthens vascular contraction and can be used for research on cardiovascular diseases such as orthostatic hypotension.
- Strengthens vascular contraction
- Increases p-AMPK and PPARδ expression in C2C12, HL1, and HepG2 cells
- Increases Ca2+ in C2C12, HL1, and HepG2 cells
- Increases maximal mitochondrial oxidative phosphorylation and ATP content in C2C12 cells
- Reduces cellular lipid content in 3T3-L1 cells
- Reduces platelet-activating factor (Paf)-induced death in mice
- Shows anti-hypotensive effects in orthostatic hypotension rat models
- Relieves hypertension in spontaneously hypertensive rat models
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Moexipril (hydrochloride) | 82586-52-5 | 98.4% | 25 MG
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Moexipril hydrochloride is an orally active inhibitor of angiotensin-converting enzyme (ACE) that becomes effective after being hydrolyzed to moexiprilat (hydrochloride). This compound demonstrates significant antihypertensive and neuroprotective effects.
- Orally active inhibitor of angiotensin-converting enzyme (ACE).
- Becomes effective after hydrolysis to moexiprilat.
- Exhibits antihypertensive and neuroprotective effects.
- High potency against plasma ACE and purified ACE from rabbit lung.
- Significantly reduces damaged neurons in a dose-dependent manner.
- Attenuates Fe2+/3+-induced neurotoxicity.
- Does not cause significant changes in apoptotic neurons.
- Does not cross the blood-brain barrier.
- Shows dose-dependent antihypertensive effects in various animal models.
- Reduces infarct area on mouse brain surface.
- Attenuates cortical infarct volume in rat brain.
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Medchemexpress LLC PhiKan 083 hydrochloride | 1050480-30-2 | 99.3% | 274.79 | 10 MG
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PhiKan 083 hydrochloride is a carbazole derivative designed to bind to the surface cavity and stabilize the Y220C p53 mutant, with a binding affinity (Kd) of 167 μM. It effectively slows down the thermal denaturation rate of the p53 mutant and has been shown to reduce cell viability in engineered variants of Ln229 cells. When used in combination with NSC 123127, it enhances pro-apoptotic activity across multiple Ln229 cell variants.
- Binds to and stabilizes Y220C p53 mutant
- Slows down thermal denaturation rate of p53 mutant
- Reduces cell viability in engineered variants of Ln229 cells
- Enhances pro-apoptotic activity when combined with NSC 123127
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Medchemexpress LLC Melitracen hydrochloride | 10563-70-9 | MFCD00242905 | >98.0% | 327.89 | C21H26ClN | 200 MG
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Melitracen hydrochloride is a research-grade tricyclic antidepressant hydrochloride salt supplied for laboratory use. It is used in pharmacological studies of monoamine neurotransmitter uptake and serotonergic (5-HT) receptor pathways. Provided as a solid for in vitro and preclinical research; not for human or veterinary use.
- Tricyclic antidepressant hydrochloride salt.
- Molecular formula C21H26ClN.
- Molecular weight 327.89.
- Purity >98.0% (HPLC).
- Available as a solid powder, commonly in 200 MG quantities.
- For research use only; not for human or veterinary use.
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Medchemexpress LLC Azasetron hydrochloride | 123040-16-4 | MFCD00209913 | 99.8% | C17H21Cl2N3O3 | 5 MG
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Azasetron hydrochloride is a benzamide derivative functioning as a potent and selective 5-HT3 receptor antagonist. It is utilized in studies concerning chemotherapy-induced nausea and vomiting (CINV).
- Potent and selective 5-HT3 receptor antagonist
- Used in studies for chemotherapy-induced nausea and vomiting (CINV)
- Purity of 99.76%
- Solid, white to off-white appearance
- Effectively penetrates skin in in vivo studies
- IC50 for 5-HT3 Receptor is 0.33 nM
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Medchemexpress LLC Endoxifen hydrochloride | 1197194-41-4 | 98.0% | 409.95 | 5 MG
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Endoxifen hydrochloride is a key active metabolite of Tamoxifen (TAM) with higher affinity and specificity to the estrogen receptor, and it also inhibits aromatase activity. It has potential for breast cancer study.
- Key active metabolite of Tamoxifen (TAM).
- Higher affinity and specificity to estrogen receptor.
- Inhibits aromatase activity.
- Potential for breast cancer study.
- Approximately 100-fold more potent as an antagonist of the ER than tamoxifen.
- Targets estrogen receptor α for degradation in breast cancer cells.
- Blocks ERA transcriptional activity and inhibits estrogen-induced breast cancer cell proliferation.
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Medchemexpress LLC Fedratinib (hydrochloride hydrate) | 1374744-69-0 | MFCD28137677 | 99.9% | 615.62 g/mol | C27H40Cl2N6O4S | 2 G
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Fedratinib hydrochloride hydrate is the dihydrochloride monohydrate salt of fedratinib, an ATP-competitive, orally active and selective JAK2 inhibitor supplied for research use. The compound is provided as a solid (white to yellow) with high reported purity and is intended for in vitro and preclinical studies; not for human therapeutic use.
- High purity (≈99.9%) as reported by supplier.
- Molecular weight 615.62 g/mol; formula C27H40Cl2N6O4S.
- Packaged in small-scale quantities, commonly available as 2 G.
- Recommended storage: solid at 4°C; in solution -20°C to -80°C.
- Potent JAK2 inhibitor with reported IC50 ≈3 nM, suitable for signaling and oncology research.
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Medchemexpress LLC SB-612111 hydrochloride | 371980-94-8 | 99.6% | 454.86 | 25 MG
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SB-612111 hydrochloride is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist. It demonstrates high affinity for hORL-1 and selectivity for μ-, κ- and δ-receptors. This compound effectively antagonizes the pronociceptive action of Nociceptin in acute pain models.
- Potent opiate receptor-like orphan receptor (ORL-1) antagonist
- High affinity for hORL-1 (Ki=0.33 nM)
- Exhibits selectivity for μ-, κ- and δ-receptors
- Antagonizes pronociceptive action of Nociceptin
- Had antihyperalgesic effects on carrageenan-induced rat paw
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Medchemexpress LLC Etifoxine hydrochloride | 56776-32-0 | MFCD00868190 | 99.9% | 337.24 g·mol⁻¹ | C17H18Cl2N2O | 10 MG
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Etifoxine hydrochloride is a non-benzodiazepine GABAergic compound used in research to modulate GABAA receptor activity. It is supplied as the hydrochloride salt for improved handling and solubility, and is commonly used in preclinical studies of anxiolytic and anticonvulsant effects.
- Acts as a positive allosteric modulator of GABAA receptors
- Hydrochloride salt form for enhanced solubility
- High purity suitable for research applications
- Available in small research pack sizes for preclinical work
- Used in studies of anxiolytic and anticonvulsant pharmacology
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Medchemexpress LLC Mozavaptan hydrochloride | 138470-70-9 | MFCD11111965 | 99.9% | 464.0 g/mol | C27H30ClN3O2 | 5MG
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Mozavaptan hydrochloride (OPC-31260 hydrochloride) is a benzazepine-derived, potent and selective vasopressin V2 receptor antagonist (reported IC50 ≈14 nM) used as a research chemical for studies of vasopressin signaling and conditions such as hyponatremia and SIADH. It is supplied as a white to off-white solid and is commonly available in small milligram quantities or as a DMSO solution for in vitro and pharmacology experiments. Molecular formula C27H30ClN3O2; molecular weight 464.0 g/mol; CAS 138470-70-9.
- High purity suitable for research (≈99.9%)
- Potent V2 receptor antagonist activity for pharmacology studies
- Available in solid and DMSO solution formats
- Compact packaging for small-scale experiments
- Standard identifiers provided for traceability
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.10% | 321.93 | 1 ML
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Leelamine hydrochloride is a tricyclic diterpene molecule extracted from the bark of pine trees. It acts as a cannabinoid receptor type 1 (CB1) agonist and an inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, independent of androgen receptor status. It also suppresses the transcriptional activity of the androgen receptor, which regulates fatty acid synthesis.
- Acts as a cannabinoid receptor type 1 (CB1) agonist
- Inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells
- Suppresses the transcriptional activity of the androgen receptor
- Extracted from the bark of pine trees
- Appears as a white to off-white solid
- Store at -20°C in sealed conditions, away from moisture
- For storage in solvent, store at -80°C for 6 months, or -20°C for 1 month in sealed conditions, away from moisture
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Medchemexpress LLC Ots186935 (hydrochloride) | 99.6% | 522.31 | 100 MG
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OTS186935 hydrochloride is a potent protein methyltransferase SUV39H2 inhibitor with an IC50 of 6.49 nM. It significantly inhibits tumor growth in mouse xenograft models without detectable toxicity and regulates the production of γ-H2AX in cancer cells. This compound has shown growth suppressive effects in human cancer cell line derived xenograft models.
- Potent SUV39H2 inhibitor
- Inhibits tumor growth in mouse xenograft models
- Regulates production of γ-H2AX in cancer cells
- Shows significant inhibition of tumor growth without detectable toxicity
- Inhibits A549 cell growth with an IC50 of 0.67 μM
- Exhibits growth suppressive effects in human cancer cell line derived xenograft models
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Medchemexpress LLC SSR180711 hydrochloride | 446031-79-4 | 99.9% | 361.66 | 25 MG
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SSR180711 hydrochloride | 446031-79-4 | 99.9% | 361.66 | 25 MG
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Medchemexpress LLC Bobcat339 hydrochloride | 2436747-44-1 | 99.6% | 334.20 | 1 ML
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Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of the TET enzyme, with IC50 values of 33 μM for TET1 and 73 μM for TET2. It is valuable in the field of epigenetics and serves as a foundation for developing new therapeutics targeting DNA methylation and gene transcription.
- Potent and selective cytosine-based inhibitor of TET enzyme.
- Useful in epigenetics research.
- Serves as a starting point for new therapeutics targeting DNA methylation and gene transcription.
- Inhibitory activity is directly related to Cu(II) content; the Bobcat339-copper mixture shows significantly higher TET inhibition than either alone.
- Significantly reduces global 5hmC levels by inhibiting TET enzyme function in HT-22 cells at 10 μM for 24 hours.
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Medchemexpress LLC Azasetron hydrochloride | 123040-16-4 | 99.8% | C17H21Cl2N3O3 | 1 ML
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Azasetron hydrochloride (Y-25130 hydrochloride) is a benzamide derivative that functions as a potent and selective 5-HT3 receptor antagonist. It is currently under study for its application in treating chemotherapy-induced nausea and vomiting (CINV).
- Potent and selective 5-HT3 receptor antagonist.
- Used to study chemotherapy-induced nausea and vomiting (CINV).
- Can effectively penetrate the skin and enter systemic circulation.
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